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Study identifier: NCT06569550 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Fatigue Alleviation Through Neuromodulating Therapy in Multiple Sclerosis

Condition: Multiple Sclerosis, Relapsing-Remitting · Fatigue  ·  Sponsor: Danish Research Centre for Magnetic Resonance

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if repetitive Transcranial Magnetic Stimulation (rTMS) of the left premotor cortex can lessen fatigue in patients with Multiple Sclerosis, and if this is a feasible intervention. It will also give further information on fatigue in Multiple Sclerosis. The main questions it aims to answer is: * Does premotor rTMS decrease fatigue symptoms in patients with Multiple Sclerosis? * Is the change in fatigue reflected in an altered balance between brain excitation and inhibition in the targeted premotor cortex? Researchers will compare real rTMS with sham rTMS (which does not stimulate with a magnetic field), to see if real rTMS works to alleviate fatigue. Participants will: * Receive real or sham rTMS for 30 minutes, 5 days in a row * Visit the clinic before and 6 days after for baseline and follow-up * Fill out on-line questionnaires 1 day and 4 weeks after the end of intervention * Undergo a total of 3 brain scans (Magnetic Resonance Imaging at ultra-high field), at baseline, end of intervention, and follow-up * Undergo lab neurophysiological measurements before and after the first intervention session * Keep a fatigue diary and wear an activity tracker in the period before and after the intervention

This description comes directly from the study's public registry record.

Talk to the study team

Hartwig R Siebner, MD, DMSc  ·  3862 6541  ·  hartwig@drcmr.dk

Sofus AD Nygaard, MD  ·  sofusadn@drcmr.dk

Always discuss trial participation with your own doctor first.

Locations (1)

Danish Research Centre for Magnetic ResonanceHvidovre, Capital Region, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT06569550